C.R. Bard Recalls
117 recalls on record · November 12, 2014 to May 27, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A300318A, SureStep" Foley Tray, Bardex" I.C., Complete Care", Drainage Bag, StatLock" Stabilization Device
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A300316A, SureStep" Foley Tray, Bardex" I.C., Complete Care", Drainage Bag, StatLock" Stabilization Device
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A300314A, SureStep" Foley Tray, Bardex" I.C., Complete Care", Drainage Bag, StatLock" Stabilization Device
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A119216M, SureStep" Foley Tray, Lubri-Sil", Urine Meter, Temperature Sensing Dual, StatLock" Stabilization Devic
Hazard: There is potential for packaging defects that may impact the sterile barrier.
April 28, 2021Medical DevicesFDA
C.R. Bard, Inc. recalls Bard Clean-Cath Intermittent Catheter, 12 French female length (catheter, urological) - Product Usage: for urological us
Hazard: The device catheter tip was cut off (no tip) and the product packaging was not fully sealed.
May 20, 2020Medical DevicesFDA
C.R. Bard Inc recalls SureStep Foley Tray System - Product Usage: Intended for use in the drainage and/or collection and/or measurement of uri
Hazard: There is potential for a white paper-type residue attached to the catheter.
February 19, 2020Medical DevicesFDA
C.R. Bard Inc recalls The Bard Intra-abdominal Pressure Monitoring Device is composed of a tubing set used for infusing fluid into the urinary
Hazard: Leaks or disconnect near the sampling port of the Intra Abdominal Pressure Monitoring Device which could lead to the potential of inaccurate readings. The measurement should be confirmed with other means, such as a new IAP system of the same kind or by choosing other diagnostic means such as but not limited to alternative systems, such as open IAP measurement options or exchanging the tubing system, which does not require invasive maneuvers.
June 27, 2018Medical DevicesFDA
C.R. Bard, Inc. recalls CritiCore Automated Urine Output and Temperature Monitor
Hazard: Issues identified with the monitor including urine output measurement errors, temperature measurement errors and undesired alarms.
June 13, 2018Medical DevicesFDA
C.R. Bard, Inc. recalls Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522)
Hazard: Foley Catheter with Incorrect Retainer Cap Print
April 18, 2018Medical DevicesFDA
C.R. Bard, Inc. recalls Bard(R) Premature Infant Feeding tube, ENFit(TM), REF EN0036430 Product Usage: BARD(R) Nasogastric Sump Tubes with
Hazard: BMD has identified that the product code/lot number combination identified above may have ineffectively fused tubing and ENFit(TM) connector.
April 18, 2018Medical DevicesFDA
C.R. Bard, Inc. recalls Bard(R) Adult/Pediatric Feeding Tube, ENFit(TM), REF EN0036420 Product Usage: BARD(R) Nasogastric Sump Tubes with E
Hazard: BMD has identified that the product code/lot number combination identified above may have ineffectively fused tubing and ENFit(TM) connector.
April 18, 2018Medical DevicesFDA
C.R. Bard, Inc. recalls Bard(R) Infant Feeding Tube, ENFit(TM), REF EN0036410 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM)
Hazard: BMD has identified that the product code/lot number combination identified above may have ineffectively fused tubing and ENFit(TM) connector.
April 18, 2018Medical DevicesFDA
C.R. Bard, Inc. recalls Bard(R) Premature Infant Feeding Tube, ENFit(TM), REF EN0036400 Product Usage: BARD(R) Nasogastric Sump Tubes with
Hazard: BMD has identified that the product code/lot number combination identified above may have ineffectively fused tubing and ENFit(TM) connector.
April 11, 2018Medical DevicesFDA
C.R. Bard, Inc. recalls Personal Intermittent Catheters- 16" and 10" lengths - 30 catheters per box, each catheter is packaged in an individual
Hazard: Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed.
April 11, 2018Medical DevicesFDA
C.R. Bard, Inc. recalls Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box, each catheter is packaged in an individual pouch. Urina
Hazard: Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed.
April 11, 2018Medical DevicesFDA
C.R. Bard, Inc. recalls HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual
Hazard: Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed.
February 21, 2018Medical DevicesFDA
C.R. Bard, Inc. recalls BARD(R) CRITICORE(R) MONITOR, Model: 000002N Series The CritiCore(R) Automated Urine Output and Temperature Monitor i
Hazard: BMD has identified that some lots of CritiCore(R) monitors may experience failures involving urine output volume measurement fluctuations, core bladder temperature measurement fluctuations and alarm errors.
February 7, 2018Medical DevicesFDA
C.R. Bard, Inc. recalls BARD UROS AUTOMATED URINE OUPTUT AND TEMPERATURE MONITOR, MODEL BK10001M The Uros(TM) Automated Urine Output and Tem
Hazard: The possibility exists that use of the Uros Automated Urine Output and Temperature Monitor may lead to the loss of urine output measurement data and/or urine output measurement inaccuracies resulting in an impact on clinical treatment decisions.
December 27, 2017Medical DevicesFDA
C.R. Bard, Inc. recalls Medivance ArcticGel Small Pad Kit - a box containing a single foil pouch, which contains a set of four (4) pads. A set o
Hazard: Hydrogel peeling from the pads.
December 27, 2017Medical DevicesFDA
C.R. Bard, Inc. recalls I-125 CE Marked QuickLink Cartridges; Sterile; Bard Brachysource Radioactive Seeds in QuickLink Cartridges Indicated
Hazard: Activity and quantity of seeds sent in shipments were incorrect.
December 13, 2017Medical DevicesFDA
C.R. Bard, Inc. recalls Arctic Sun ArcticGel Pads - Medium, Product Code 317-07
Hazard: Label on product box contains the incorrect reference #317-09 while the shelf box label with barcode and the internal foil pouch label are correctly labeled with product code 317-07 and lot number NDAR0462.
October 4, 2017Medical DevicesFDA
C.R. Bard, Inc. recalls Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female, 14 FR (30/box), Rx Only intended for urinary bladde
Hazard: Specific lots labeled as an Antibacterial Hydrophilic Intermittent Catheter may lack the hydrophilic coating.
August 23, 2017Medical DevicesFDA
C.R. Bard, Inc. recalls Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US
Hazard: Potential failure of the Arctic Sun 5000 Temperature Management System may occur when the continued use is in excess of 2000 system hours without preventive maintenance.
August 16, 2017Medical DevicesFDA
C.R. Bard, Inc. recalls BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension, Extension Tube and Latex Straps, 19 oz. Packaged as
Hazard: Customer complaint of a cut in the side of the leg bag, indicating a potential breach of the product's sterile barrier.
April 26, 2017Medical DevicesFDA
C.R. Bard, Inc. recalls SURESTEP Tray, Bardex I.C. Complete Care Drainage Bag, 2000 ml Drainage Bag, 16 Fr., Sterile.
Hazard: Misbranded: Product labeled, Not made with natural rubber latex, may in fact contain natural rubber latex.
January 18, 2017Medical DevicesFDA
C.R. Bard, Inc. recalls SURESTEP Tray, BARDEX I.C. COMPLETE CARE, Urine Meter, Temperature STATLOCK Stabilization Device
Hazard: The product contained a latex catheter instead of a silicone catheter.
December 21, 2016Medical DevicesFDA
C.R. Bard, Inc. recalls BARDIA¿ 60cc Piston Irrigation Syringe, Sterile, Rx Only, The BARD¿ Syringe is available in a single use plastic design
Hazard: Package Defect: Products may be at risk for having a slit defect on the package and that may affect the product sterility.
December 21, 2016Medical DevicesFDA
C.R. Bard, Inc. recalls BARD¿ Piston Syringe, 60cc, Rx Only, Sterile, The BARD¿ Syringe is available in a single use plastic design which featur
Hazard: Package Defect: Products may be at risk for having a slit defect on the package and that may affect the product sterility.
December 21, 2016Medical DevicesFDA
C.R. Bard, Inc. recalls BARD¿ 70cc Piston Syringe with Catheter Tip, Luer Adapter and Cap, Rx Only, The BARD¿ Syringe is available in a single u
Hazard: Package Defect: Products may be at risk for having a slit defect on the package and that may affect the product sterility.
December 21, 2016Medical DevicesFDA
C.R. Bard, Inc. recalls BARD¿ Irrigation, Syringe 70cc With Resectoscope Tip, Catheter Tip, Luer Adapter And Cap, Rx Only, Sterile, The BARD¿
Hazard: Package Defect: Products may be at risk for having a slit defect on the package and that may affect the product sterility.